Primary Device ID | 00817770022374 |
NIH Device Record Key | 58d6a97b-796a-4b0a-90ac-0b558a8d4692 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MicroBlender |
Version Model Number | Low Flow NIST |
Catalog Number | R219P24-002 |
Company DUNS | 169911828 |
Company Name | MAXTEC, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00817770022374 [Primary] |
BZR | Mixer, Breathing Gases, Anesthesia Inhalation |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-06-16 |
Device Publish Date | 2023-06-08 |
00817770021629 | High Flow with NIST Fitting |
00817770020714 | Low Flow |
00817770022374 | Low Flow MicroBlender with Flowmeters (China Labeled) |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MICROBLENDER 76416181 3545461 Dead/Cancelled |
Maguire Products, Inc. 2002-05-31 |
MICROBLENDER 73361948 not registered Dead/Abandoned |
WAUGH CONTROLS CORPORATION 1982-04-28 |